ncbi / magicblastLinks
☆36Updated 8 months ago
Alternatives and similar repositories for magicblast
Users that are interested in magicblast are comparing it to the libraries listed below
Sorting:
- Whole Exome/Whole Genome Sequencing alignment pipeline☆28Updated last year
- small RNA analysis from NGS data☆37Updated last year
- Master of Pores 2☆23Updated last year
- De novo transcriptome assembler for short reads☆64Updated 7 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆59Updated 8 years ago
- A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies☆35Updated last year
- Malleable All-seeing Journal Of Research Artifacts☆35Updated 2 years ago
- Hitting associations with k-mers☆44Updated 3 years ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆46Updated 6 years ago
- A collection of publications on comparison of high-throughput sequencing technologies.☆27Updated 3 weeks ago
- This repository contains the source code of JUDI, a workflow management system for developing complex bioinformatics software with many p…☆33Updated 4 years ago
- Test data for MultiQC.☆24Updated last week
- Maximum likelihood demultiplexing☆50Updated 10 months ago
- Deprecated see https://github.com/MHH-RCUG/nf_wochenende : A whole Genome/Metagenome Sequencing Alignment Pipeline in Python3☆37Updated 3 years ago
- Please consider using/contributing to https://github.com/nf-core/sarek☆41Updated 4 years ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- conda recipes for genomic data☆84Updated 4 years ago
- This repository has been archived, currently maintained version is at https://github.com/iii-companion/companion☆21Updated 4 years ago
- deSALT - De Bruijn graph-based Spliced Aligner for Long Transcriptome reads☆44Updated 3 years ago
- Genome guided re-segmention and visualization for raw nanopore sequencing data.☆47Updated 7 years ago
- An easy to use and comprehensive python package which aids in the analysis and visualization of orthologous genes. 🐵☆28Updated 3 weeks ago
- Reference-free variant discovery in large eukaryotic genomes☆41Updated 4 years ago
- PERF is an Exhaustive Repeat Finder☆34Updated 4 years ago
- mtDNA Variant Caller☆35Updated last year
- Assembler for raw de novo genome assembly of long uncorrected reads.☆36Updated 6 years ago
- Nextflow workflow for automatic repeat detection, classification and masking☆13Updated 7 years ago
- Find Unique genomic Regions☆32Updated 2 months ago
- Error correction for Illumina RNA-seq reads☆67Updated last year
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 3 years ago
- full taxonomer cython repository☆22Updated 6 years ago